A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041262



Internal ID19130481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20011690..21997806hg38UCSC Ensembl
Innerchr15:20216943..22285757hg19UCSC Ensembl
Innerchr15:18476957..19787121hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg381986117
hg192068815
hg181310165
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2190n100
Supporting Variantsnssv3536998, nssv3537002, nssv3537000, nssv3536996, nssv3536997, nssv3537001, nssv3715779, nssv3536999, nssv3715777, nssv3536995, nssv3536994, nssv3715778
Samples
Known GenesCHEK2P2, CT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, LOC727924, NBEAP1, NF1P2, POTEB, POTEB2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1041262
Frequency
Sample Size11257
Observed Gain4
Observed Loss8
Observed Complex0
Frequencyn/a


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